𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Glucose-6-phosphate dehydrogenase (G6PD) Guantánamo and G6PD Caujerí: Two new glucose-6-phosphate dehydrogenase-deficient variants found in Cuba

✍ Scribed by A. Gutiérrez; M. García; M. Estrada; I. Quintero; R. González

Publisher
Springer
Year
1987
Tongue
English
Weight
359 KB
Volume
25
Category
Article
ISSN
0006-2928

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Glucose-6-phosphate dehydrogenase (G6PD)
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese
✍ O. Ainoon; J. Joyce; N.Y. Boo; S.K. Cheong; Z.A. Zainal; N.H. Hamidah 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 31 KB 👁 2 views

We screened 38 G6PD-deficient male Chinese neonates for known G6PD mutations using established PCR-based techniques. We found 50.0% (19 of 38) were mutation 1376G>T, 34.2% (13 of 38) were mutation 1388G>A, 5.2% (2 of 38 ) were mutation 95A>G and 2.2% (1 of 38) was mutation 1024C>T. In 7% (3 of 38) o

Glucose-6-phosphate dehydrogenase (G6PD)
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays
✍ O. Ainoon; Y.H. Yu; A.L. Amir Muhriz; N.Y. Boo; S.K. Cheong; N.H. Hamidah 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 50 KB

We performed DNA analysis using cord blood samples on 86 male Malay neonates diagnosed as G6PD deficiency in the National University of Malaysia Hospital by a combination of rapid PCR-based techniques, single-stranded conformation polymorphism analysis (SSCP) and DNA sequencing. We found 37.2% were

A new glucose 6 phosphate dehydrogenase
A new glucose 6 phosphate dehydrogenase variant, G6PD Sinnai (34 G→T)
✍ Renzo Galanello; Daniela Loi; Carla Sollaino; Sandra Dessì; Antonio Cao; Maria A 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 31 KB 👁 2 views

In this paper we report a male infant heterozygous for -thalassemia with a mild glucose 6 phosphate dehydrogenase deficiency. The molecular basis of this new Class III G6PD variant is a G->T mutation at nucleotide 34 in the exon 2, which predicts a Val->Leu aminoacid substitution at codon 12. We des